Arm and Hammer Spinbrush Dual Action Powered Toothbrush Spinbrush Pro… — Class II medical device recall Z-0859-2012
Terminated recall by Church & Dwight Inc, reported 2012-08-08. Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard
| Recall number | Z-0859-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Church & Dwight Inc, Princeton, NJ, United States |
| Recall initiated | 2011-12-22 |
| Classified | 2012-07-27 |
| Reported by FDA | 2012-08-08 |
| Terminated | 2015-04-14 |
| Quantity | 15.589 million |
Product
Arm and Hammer Spinbrush Dual Action Powered Toothbrush Spinbrush Pro Whitening Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.
Reason for recall
Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0859-2012. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.